Canonical Allele Identifier: CA1771650807
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24952553G= , CM000670.2:g.24952553G= GRCh38
NC_000008.10:g.24810066G= , CM000670.1:g.24810066G= GRCh37
NC_000008.9:g.24865983G= NCBI36
NG_008492.1:g.9065C= , LRG_259:g.9065C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.2:c.*257C= MANE Select ENSP00000482169.2:n.*257C=
ENST00000610854.1:c.*257C= ENSP00000482169.1:n.*257C=
ENST00000619417.1:c.*754C= ENSP00000483690.1:n.*754C=
NM_006158.4:c.*257C= , LRG_259t1:c.*257C= NP_006149.2:n.*257C=
NM_006158.5:c.*257C= MANE Select NP_006149.2:n.*257C=